CAS 56-91-7
:Ácido 4-(aminometil)benzoico
Descripción:
Ácido 4-(aminometil)benzoico, también conocido como ácido p-aminobenzilcarboxílico, es un aminoácido aromático caracterizado por la presencia de un grupo amino (-NH2) y un grupo ácido carboxílico (-COOH) unidos a un anillo bencénico. Este compuesto típicamente aparece como un sólido cristalino blanco a blanco sucio y es soluble en agua, reflejando sus grupos funcionales polares. Tiene un punto de fusión que varía dependiendo de la pureza y la forma, y es conocido por su papel en diversas síntesis químicas y aplicaciones, particularmente en productos farmacéuticos y como un bloque de construcción en química orgánica. El grupo amino puede participar en varias reacciones, incluyendo la formación de amidas y reacciones de acoplamiento, lo que lo hace versátil en rutas sintéticas. Además, Ácido 4-(aminometil)benzoico puede exhibir actividad biológica, lo que puede ser de interés en química medicinal. Su número CAS, 56-91-7, es un identificador único que facilita su reconocimiento en bases de datos químicas y marcos regulatorios.
Fórmula:C8H9NO2
InChI:InChI=1S/C8H9NO2/c9-5-6-1-3-7(4-2-6)8(10)11/h1-4H,5,9H2,(H,10,11)
Clave InChI:InChIKey=QCTBMLYLENLHLA-UHFFFAOYSA-N
SMILES:C(O)(=O)C1=CC=C(CN)C=C1
Sinónimos:- 4-(Aminomethyl)benzoic acid
- 4-Carboxybenzylamine
- Benzoic acid, 4-(aminomethyl)-
- Benzylamine-4-carboxylic acid
- Gumbix
- NSC 41629
- Pamba
- Styptopur
- p-(Aminomethyl)benzoic acid
- p-Carboxybenzylamine
- p-Toluic acid, α-amino-
- α-Amino-p-toluic acid
- 4-Aminomethylbenzoic acid
- 4-CARBOXYLBENZYLAMINE
- H-4-AMB-OH
- AMINOMETHYL BENZOIC ACID
- NH2-CH2-PH(4)-COOH
- H-(4)AMBZ-OH
- Aminomethylbenzoic acid CP2000
- TIMTEC-BB SBB006704
- Benzoic acid, 4-(aminomethyl)-(9CI)
- -Amino-p-toluicacid
- 4-Aminomethylbenzonium acid
- p-Aminomethylbenzoic
- 4-(AMINOMETHYL)BENZOIC ACIDTRANEXAMIC ACID
- RARECHEM AL BW 0005
- Ver más sinónimos
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Encontrado 14 productos.
4-(Aminomethyl)benzoic acid, 97%
CAS:<p>4-(Aminomethyl)benzoic acid acts as an unnatural amino acid derivative. It is also used as a type 2 antifibrinolytic agent. Further, it reacts with 2-methyl-isothiourea sulfate to prepare 4-guanidinomethylbenzoic acid. This Thermo Scientific Chemicals brand product was originally part of the Alfa Ae</p>Fórmula:C8H9NO2Pureza:97%Forma y color:White to cream, PowderPeso molecular:151.174-(Aminomethyl)benzoic acid
CAS:4-(Aminomethyl)benzoic acid (PAMBA), an antifibrinolytic, is an unnatural amino acid derivative.Fórmula:C8H9NO2Pureza:99.55% - 99.64%Forma y color:White To Light Yellow Crystal PowderPeso molecular:151.16Tranexamic Acid EP Impurity D
CAS:Fórmula:C8H9NO2Forma y color:White To Off-White SolidPeso molecular:151.174-(Aminomethyl)benzoic acid
CAS:Fórmula:C8H9NO2Pureza:(HPLC) ≥ 98.0%Forma y color:White to off-white powderPeso molecular:151.164-(Aminomethyl)benzoic acid
CAS:4-(Aminomethyl)benzoic acidFórmula:C8H9NO2Pureza:98%Forma y color: white solidPeso molecular:151.16g/mol4-(Aminomethyl)benzoic Acid
CAS:Fórmula:C8H9NO2Pureza:>97.0%(T)(HPLC)Forma y color:White to Light yellow powder to crystalPeso molecular:151.174-Aminomethylbenzoic Acid
CAS:Producto controladoFórmula:C8H9NO2Forma y color:NeatPeso molecular:151.164-(Aminomethyl)benzoic Acid
CAS:Producto controlado<p>Impurity Tranexamic EP Impurity D<br>Applications 4-(Aminomethyl)benzoic Acid (Tranexamic EP Impurity D) is a type 2 antifibrinolytic agent.<br>References Markwardt, F., et al.: Prog. Fibrinolysis. 5, 178 (1981); Markswardt, F.. et al.: Thrombosis. Res., 9, 143 (1976);<br></p>Fórmula:C8H9NO2Forma y color:WhitePeso molecular:151.164-Aminomethylbenzoic acid
CAS:<p>4-Aminomethylbenzoic acid (4AMBA) is a metabolite that is formed from the amino acid methionine. It has been shown to inhibit the growth of prostate cancer cells in vitro and in vivo. 4-Aminomethylbenzoic acid inhibits the activity of polymerase chain reaction (PCR), which is an enzyme that catalyzes DNA replication. The hydroxyl group on 4-aminomethylbenzoic acid reacts with one of the phosphate groups on DNA, forming a covalent bond and inhibiting DNA synthesis. This inhibition occurs at the step called initiation, where DNA synthesis begins by binding of RNA polymerase to a specific sequence of DNA. In addition, 4-aminomethylbenzoic acid also inhibits the activity of x-ray diffraction data, which is an enzyme that catalyzes RNA transcription. Histological analysis shows that 4-aminomethylbenzoic acid causes congestive heart</p>Fórmula:C8H9NO2Pureza:Min. 98 Area-%Forma y color:White PowderPeso molecular:151.16 g/mol













